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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03309280
Other study ID # VACC Study
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 9, 2017
Est. completion date June 1, 2018

Study information

Verified date January 2020
Source Astes
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to determine which factors could be at risk of delayed extubation after cardiac surgery.


Description:

The aim of this study is to determine which factors could be at risk of delayed extubation after cardiac surgery. Several parameters of ventilation and infusion were recorded during surgery. A statistical analysis will be performed to determine if one of many of these are significant. The investigator does not assign specific interventions to the study participants, so the present study is observational and not interventional.


Recruitment information / eligibility

Status Completed
Enrollment 132
Est. completion date June 1, 2018
Est. primary completion date April 3, 2018
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- All patients for elective cardiac surgery

Exclusion Criteria:

- Emergency procedures

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Duration of intubation
Time between intubation in the operating room and exhumation in the Intensive Care Unit.
Diagnostic Test:
Evolution of the renal function
Evolution of the renal function in the next two days

Locations

Country Name City State
Belgium Clinique Saint-Luc de Bouge Bouge Namur

Sponsors (1)

Lead Sponsor Collaborator
Astes

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time of extubation Time when extubation is performed 2 Days
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